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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Hemoglobinopathies > Thalassemia
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemoglobinopathies > Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Thalassemia
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Thalassemia

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Thalassemia  

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Tipo

  • mesh:Descriptor

Definición

  • A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • Thalassemias

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URI

http://data.loterre.fr/ark:/67375/JVR-JF62H9M7-V

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